A CQV Engineer is required by Career Wise Recruitment for our multinational pharmaceutical client in Dublin for a full time onsite, initial 12-month contract role, to start in the new year.
The CQV Engineer will lead CQV work for a number of projects including bulk processing, fill/pack lines and utilities/facilities upgrades.
THE ROLE: Develop and execute commissioning, qualification, and validation protocols for equipment, utilities, and processes.
Prepare detailed documentation including URS, FRS, IOQ, and PQ protocols.
Coordinate and perform risk assessments and impact assessments for new and existing systems.
Collaborate with cross-functional teams to ensure timely project delivery.
Troubleshoot and resolve issues that arise during the CQV process.
Ensure compliance with c GMP, FDA, and other relevant regulations and guidelines.
Maintain accurate and up-to-date documentation and reports.
Provide training and guidance to operational staff on validated systems and procedures.
REQUIREMENTS: Bachelors Degree (L8) in Engineering/Science/Technical.
Minimum of 5+ years relevant professional experience within the pharmaceutical industry.
Experience in process, fill/pack and utility systems of interest.
Please call Laura Gallagher today for further information on or email: Career Wise Recruitment (In Search of Excellence) Established in 1999, Career Wise Recruitment specialises in recruitment of management and technical professionals for the life sciences, ICT, engineering, food and agri sectors.
We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway, Mayo and Dublin.
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Skills: CQV Engineer